Canonical Allele Identifier: CA1918678355

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362117A= , CM000672.2:g.71362117A=	GRCh38
NC_000010.10:g.73121874A= , CM000672.1:g.73121874A=	GRCh37
NC_000010.9:g.72791880A=	NCBI36
NG_017066.1:g.47865A=
NG_017066.2:g.47859A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2413A=
ENST00000373189.6:c.937A= MANE Select	ENSP00000362285.5:p.Thr313=
ENST00000479577.2:c.703A=	ENSP00000493995.1:p.Thr235=
ENST00000642198.1:c.*509A=	ENSP00000494827.1:n.*509A=
ENST00000642772.1:c.*94+5874A=	ENSP00000495041.1:n.*94+5874A=
ENST00000643042.1:c.558A=	ENSP00000496674.1:n.558A=
ENST00000643619.1:c.*520A=	ENSP00000494378.1:n.*520A=
ENST00000643752.1:c.*263A=	ENSP00000495000.1:n.*263A=
ENST00000644088.1:c.*258A=	ENSP00000494066.1:n.*258A=
ENST00000644591.1:c.*263A=	ENSP00000496664.1:n.*263A=
ENST00000644895.1:c.*99+5874A=	ENSP00000493872.1:n.*99+5874A=
ENST00000645345.1:c.*509A=	ENSP00000495859.1:n.*509A=
ENST00000647524.1:c.*520A=	ENSP00000495077.1:n.*520A=
ENST00000373189.5:c.937A=	ENSP00000362285.5:p.Thr313=
ENST00000469204.1:n.434A=
NM_001174098.1:c.*166A=	NP_001167569.1:n.*166A=
NM_018344.5:c.937A=	NP_060814.4:p.Thr313=
NR_033413.1:n.911A=
NR_033414.1:n.684A=
XM_006717910.2:c.703A=	XP_006717973.1:p.Thr235=
NM_001363518.1:c.703A=	NP_001350447.1:p.Thr235=
XM_017016377.2:c.499A=	XP_016871866.1:p.Thr167=
XM_017016378.2:c.319A=	XP_016871867.1:p.Thr107=
NM_018344.6:c.937A= MANE Select	NP_060814.4:p.Thr313=
NM_001174098.2:c.*166A=	NP_001167569.1:n.*166A=
NM_001363518.2:c.703A=	NP_001350447.1:p.Thr235=
NR_033413.2:n.905A=
NR_033414.2:n.678A=